Severe Early‐Onset Parkinsonian Syndrome Caused by PLA2G6 Heterozygous Variants-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Severe Early‐Onset Parkinsonian Syndrome Caused by PLA2G6 Heterozygous Variants

Published:2021-05-06 Issue:5 Volume:8 Page:794-796
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Mov Disord Clin Pract

Author:

Oliveira Pérola¹^ORCID,Montanaro Vinicius¹,Carvalho Daniel²,Martins Bernardo³,Ferreira Alessandra²,Cardoso Francisco⁴^ORCID

Affiliation:

1. Department of Neurology SARAH Network of Rehabilitation Hospitals Brasília Brazil

2. Department of Genetic SARAH Network of Rehabilitation Hospitals Brasília Brazil

3. Department of Radiology SARAH Network of Rehabilitation Hospitals Brasília Brazil

4. Movement Disorders Unit, Neurology Service, Department of Clinical Medicine Federal University of Minas Gerais Belo Horizonte Brazil

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13230

Reference10 articles.

1. PLA2G6-Associated Neurodegeneration (PLAN): Review of Clinical Phenotypes and Genotypes

2. Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism

3. Genotype-phenotype correlations of adult-onset PLA2G6-associated Neurodegeneration: case series and literature review

4. PLA2G6 gene mutation in autosomal recessive early-onset parkinsonism in a Chinese cohort

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A novel variant of PLA2G6 gene related early-onset parkinsonism: a case report and literature review;Frontiers in Neurology;2024-04-18

2. Frequency of Hereditary and GBA1‐Related Parkinsonism in Latin America: A Systematic Review and Meta‐Analysis;Movement Disorders;2023-11-03

3. Generation of feeder-independent transgene-free iPSC lines from a young-onset Parkinson’s disease (YOPD) patient with a homozygous PLA2G6: c.2222G>A (p. Arg741Gln) mutation (NCBSi003-A) and unaffected heterozygous parent (NCBSi004-A);Stem Cell Research;2023-03

4. Case Report: A case of PLA2G6 gene-related early-onset Parkinson's disease and review of literature;Frontiers in Neuroscience;2022-12-09

5. Reply to: Juvenile PLA2G6 ‐parkinsonism due to Indian ‘Asian’ p.R741Q mutation, and response to STN DBS;Movement Disorders;2022-02-13

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3